Canonical Allele Identifier: CA804782913

Gene: SLC6A3

Linked Data

• dbSNP Id: rs1159224830
• MyVariant Identifiers: chr5:g.1414654_1414655insACC (hg19) ; chr5:g.1414539_1414540insACC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1414544_1414546dup , CM000667.2:g.1414544_1414546dup	GRCh38
NC_000005.9:g.1414659_1414661dup , CM000667.1:g.1414659_1414661dup	GRCh37
NC_000005.8:g.1467659_1467661dup	NCBI36
NG_015885.1:g.35887_35889dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270349.12:c.1156+149_1156+151dup MANE Select	ENSP00000270349.9:n.1156+149_1156+151dup
ENST00000270349.11:c.1156+149_1156+151dup	ENSP00000270349.9:n.1156+149_1156+151dup
NM_001044.4:c.1156+149_1156+151dup	NP_001035.1:n.1156+149_1156+151dup
NM_001044.5:c.1156+149_1156+151dup MANE Select	NP_001035.1:n.1156+149_1156+151dup